chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2117991497117991498CT10GENICpossibly homozygous563622099
2117992660117992661GA9GENICheterozygous564680112
2117993091117993092CT6GENIChomozygous563622100
2117993850117993851AAT2GENIChomozygous708055086
2117994686117994687AG9GENIChomozygous564680113
2117994875117994876TG7GENICpossibly homozygous563622101
2117994890117994891TC6GENICheterozygous563622102
2117995042117995043T-4GENIChomozygous708055088
2117996552117996553AG3GENIChomozygous563622103
2117996858117996859CT6GENIChomozygous564680114
2117997021117997022GT3GENIChomozygous564680115
2117997039117997040GT1GENIChomozygous564680116
2117997043117997044CA1GENIChomozygous564680117
2117997044117997045TC1GENIChomozygous564680118
2117997053117997054CG1GENIChomozygous564680119
2117998262117998263CA3GENICheterozygous563622104
2117998342117998343AG4GENICheterozygous563622105
2117998363117998364AG3GENIChomozygous563622106
2117998368117998369TG3GENIChomozygous563622107
2117998377117998378AG3GENIChomozygous563622108
2117998380117998381AG4GENIChomozygous564680120
2117998383117998384TG4GENIChomozygous563622109
2117998444117998445A-15GENIChomozygous708055089
2117998533117998534GA5GENICheterozygous563622110
2117998771117998772GA18GENIChomozygous563622111
2117998994117998995TC20GENIChomozygous563622112
2117999795117999796AG7GENICpossibly homozygous563622113
2117999887117999888TG17GENIChomozygous563622114
2118000476118000477AG11GENIChomozygous563622115
2118001569118001570CT28GENICpossibly homozygous563622116
2118001690118001691CG19GENIChomozygous563622117
2118001805118001806CG23GENICpossibly homozygous563622118
2118004282118004283GA19GENICpossibly homozygous563622119
2118004781118004782AT3GENIChomozygous563622120
2118005113118005114CG19GENIChomozygous563622121
2118005418118005419GA18GENIChomozygous563622122
2118007021118007022CT17GENIChomozygous563622123